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  4. NDC Product Code: 49781-083 Leader Extra Strength Medicated Pain Relief Patch

NDC 49781-083 Leader Extra Strength Medicated Pain Relief Patch

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 49781-083?
  4. Leader Extra Strength Medicated Pain Relief Patch Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
49781-083
Proprietary Name:
Leader Extra Strength Medicated Pain Relief Patch
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cardinal Health
Labeler Code:
49781
Product Label ID:
f7a550a0-1c0d-40df-b7e6-734ac4f999f3
Start Marketing Date: [9]
03-25-2014
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

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Product Details

What is NDC 49781-083?

The NDC code 49781-083 is assigned by the FDA to the product Leader Extra Strength Medicated Pain Relief Patch which is product labeled by Cardinal Health. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 49781-083-70 1 patch in 1 box / 1 g in 1 patch, 49781-083-71 5 patch in 1 box / 1 g in 1 patch. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Leader Extra Strength Medicated Pain Relief Patch?

Directionsadults and children 12 years oldpeel off protective backing and apply sticky side to affected areashould be used up to 8 hoursshould be used no more than 3 times a daychildren under 12 years of age consult a doctor

Which are Leader Extra Strength Medicated Pain Relief Patch UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Leader Extra Strength Medicated Pain Relief Patch Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Leader Extra Strength Medicated Pain Relief Patch?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".